Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110602147A>G , CM000672.2:g.110602147A>G | GRCh38 |
| NC_000010.10:g.112361905A>G , CM000672.1:g.112361905A>G | GRCh37 |
| NC_000010.9:g.112351895A>G | NCBI36 |
| NG_012217.1:g.39457A>G , LRG_774:g.39457A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.5307A>G | ||
| ENST00000685743.1:n.2782A>G | ||
| ENST00000686057.1:n.1425A>G | ||
| ENST00000689321.1:n.2037A>G | ||
| ENST00000689986.1:n.863A>G | ||
| ENST00000361804.5:c.3074A>G MANE Select | ENSP00000354720.5:p.Lys1025Arg | |
| ENST00000361804.4:c.3074A>G | ENSP00000354720.4:p.Lys1025Arg | |
| NM_005445.3:c.3074A>G , LRG_774t1:c.3074A>G | NP_005436.1:p.Lys1025Arg | |
| NM_005445.4:c.3074A>G MANE Select | NP_005436.1:p.Lys1025Arg |